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Items: 17

1.

Control of mammalian circadian rhythm by CKIepsilon-regulated proteasome-mediated PER2 degradation.

Eide EJ, Woolf MF, Kang H, Woolf P, Hurst W, Camacho F, Vielhaber EL, Giovanni A, Virshup DM.

Mol Cell Biol. 2005 Apr;25(7):2795-807.

2.

The circadian regulatory proteins BMAL1 and cryptochromes are substrates of casein kinase Iepsilon.

Eide EJ, Vielhaber EL, Hinz WA, Virshup DM.

J Biol Chem. 2002 May 10;277(19):17248-54. Epub 2002 Mar 1.

3.

Nuclear export of mammalian PERIOD proteins.

Vielhaber EL, Duricka D, Ullman KS, Virshup DM.

J Biol Chem. 2001 Dec 7;276(49):45921-7. Epub 2001 Oct 8.

4.

Casein kinase I: from obscurity to center stage.

Vielhaber E, Virshup DM.

IUBMB Life. 2001 Feb;51(2):73-8. Review.

5.

Nuclear entry of the circadian regulator mPER1 is controlled by mammalian casein kinase I epsilon.

Vielhaber E, Eide E, Rivers A, Gao ZH, Virshup DM.

Mol Cell Biol. 2000 Jul;20(13):4888-99.

6.

Germline origins in the human F9 gene: frequent G:C-->A:T mosaicism and increased mutations with advanced maternal age.

Ketterling RP, Vielhaber E, Li X, Drost J, Schaid DJ, Kasper CK, Phillips JA 3rd, Koerper MA, Kim H, Sexauer C, Gruppo R, Ambriz R, Paredes R, Sommer SS.

Hum Genet. 1999 Dec;105(6):629-40.

PMID:
10647899
7.

Regulation of casein kinase I epsilon and casein kinase I delta by an in vivo futile phosphorylation cycle.

Rivers A, Gietzen KF, Vielhaber E, Virshup DM.

J Biol Chem. 1998 Jun 26;273(26):15980-4.

8.

Molecular epidemiology of factor IX germline mutations in Mexican Hispanics: pattern of mutation and potential founder effects.

Thorland EC, Weinshenker BG, Liu JZ, Ketterling RP, Vielhaber EL, Kasper CK, Ambriz R, Paredes R, Sommer SS.

Thromb Haemost. 1995 Dec;74(6):1416-22.

PMID:
8772212
9.

The rates of G:C-->T:A and G:C-->C:G transversions at CpG dinucleotides in the human factor IX gene.

Ketterling RP, Vielhaber E, Sommer SS.

Am J Hum Genet. 1994 May;54(5):831-5.

10.

"Cryptic" dinucleotide polymorphism in the 3' region of the factor IX gene shows substantial variation among different populations.

Sommer SS, Tillotson VL, Vielhaber EL, Ketterling RP, Dutton CM.

Hum Genet. 1994 Mar;93(3):357-8.

PMID:
8125492
11.

The rates and patterns of deletions in the human factor IX gene.

Ketterling RP, Vielhaber EL, Lind TJ, Thorland EC, Sommer SS.

Am J Hum Genet. 1994 Feb;54(2):201-13.

12.

Mutation detection, prenatal testing, and delineation of the germline origin in a family with sporadic hemophilia B and no living hemophiliacs.

Vielhaber E, Sommer SS, Freedenberg D.

Am J Med Genet. 1994 Jan 15;49(2):257-8. No abstract available.

PMID:
8116680
13.

Identification of mutations in four hemophilia B patients of Turkish origin, including a novel deletion of base 6411.

Cağlayan SH, Vielhaber E, Gürsel T, Aktuğlu G, Sommer SS.

Hum Mutat. 1994;4(2):163-5. No abstract available.

PMID:
7981722
14.

A mutation in the 3' untranslated region of the factor IX gene in four families with hemophilia B.

Vielhaber E, Jacobson DP, Ketterling RP, Liu JZ, Sommer SS.

Hum Mol Genet. 1993 Aug;2(8):1309-10. No abstract available.

PMID:
8401514
15.

The pattern of spontaneous germ-line mutation: relative rates of mutation at or near CpG dinucleotides in the factor IX gene.

Bottema CD, Ketterling RP, Vielhaber E, Yoon HS, Gostout B, Jacobson DP, Shapiro A, Sommer SS.

Hum Genet. 1993 Jun;91(5):496-503.

PMID:
8314564
16.

Germline mutations in the factor IX gene: a comparison of the pattern in Caucasians and non-Caucasians.

Gostout B, Vielhaber E, Ketterling RP, Yoon HS, Bottema CD, Kasper CK, Koerper MA, Sommer SS.

Hum Mol Genet. 1993 Mar;2(3):293-8.

PMID:
8499919
17.

Germ-line origins of mutation in families with hemophilia B: the sex ratio varies with the type of mutation.

Ketterling RP, Vielhaber E, Bottema CD, Schaid DJ, Cohen MP, Sexauer CL, Sommer SS.

Am J Hum Genet. 1993 Jan;52(1):152-66.

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